HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-1-benzofuran-7-carbaldehyde → HCID 15428564, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-1-benzofuran-7-carbaldehyde | HCID 21220840 | — |
| Reactant | 1-methyl-5-(tributylstannyl)-1H-1,2,3-triazole | HCID 22609826 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 15428564 | HCID 15428564 | 251.5% |
Reaction Steps
A mixture of 5-bromo-benzofuran-7-carbaldehyde (0.315 g), 1-methyl-5-tributylstannanyl-1H-[1,2,3]-triazole (0.525 g) and bis(triphenylphosphine)palladium (II) chloride (0.05 g) in toluene (7 ml) was stirred and refluxed under nitrogen for 5 h. The cooled mixture was diluted with 8% sodium bicarbonate (30 ml) and extracted with ethyl acetate (3×25 ml). The combined extracts were dried (MgSO4) and the solvent removed in vacuo to give a yellow solid (0.8 g). Purification by FCC, eluting with ethyl acetate-hexane, then ethyl acetate gave a cream solid, which was crystallised from ethyl acetate to give the title compound as pale green crystals (0.18 g), m.p. 180-2°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935972 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-b6921322051d43b49cf900e5ded90a2e |
| Source note | uspto-grants-1999_08 |